K-number	K012768
Device name	HEMOSIL RECOMBI PLASTIN
Applicant	Instrumentation Laboratory CO
Product code	GJS
Device class	Class II
Decision date	Sep 18, 2001
Decision	Substantially Equivalent
Regulation	864.7750

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View the full FDA submission: accessdata.fda.gov

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HEMOSIL RECOMBI PLASTIN

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